Teilstruktursuche

874408

—
Reaction #86678
solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86679
solid
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86680
solid
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86681
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86682
title compound
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86683
Solid
Ausbeute 167.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86684
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86685
solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86686
solid
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86687
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86688
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86689
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86690
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #428819
6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #428820
6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin -1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #428821
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #428822
Solid
Ausbeute 236.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #961222
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1 (2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #961223
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #961224
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
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